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Macular Degeneration, Retina/Vitreous
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Increasing Lutein Consumption – Are all Luteins Alike?

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Published Online: Jan 24th 2012 European Ophthalmic Review, 2011;5(2):127-129 DOI: http://doi.org/10.17925/EOR.2011.05.02.127
Authors: Samanta Maci
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Abstract
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Abstract:
Overview

Epidemiological and intervention studies suggest that lutein may act as a nutritional factor able to modulate visual performance as well as the processes implicated in the pathogenesis and progression of degenerative eye diseases. Since lutein cannot be synthesised by the body, and daily dietary consumption is generally below the level of intake found to be beneficial in clinical studies, increased consumption – through diet or supplementation – is recommended. The prerequisites for lutein to benefit the eye are: release from the food or food supplement matrix in which it is included; absorption by the intestinal cell; presence in adequate concentrations in serum; and deposition of serum lutein into the macula of the eye. Not all lutein ingredients are alike so, when recommending eye supplements to patients, in addition to looking for safe products, it is critical to ensure that the lutein ingredient used is absorbed properly by the body and has proven its efficacy in clinical trials.

Support: The publication of this article was funded by Kemin Health.

Keywords

Lutein, zeaxanthin, macular pigment, dietary sources, absorption, lutein supplementation, bioavailability

Article:

Growing scientific evidence supports the beneficial role of lutein in eye health. Lutein is found, together with its isomer zeaxanthin, in almost all the structures of the eye. Lutein and zeaxanthin are the only two dietary carotenoids selectively concentrated in the lens and in the macula, where they are the key components of the macular pigment (MP). An additional carotenoid present in the macula, meso-zeaxanthin, is a stereoisomer of lutein and zeaxanthin that is not naturally found in the human diet.


Growing scientific evidence supports the beneficial role of lutein in eye health. Lutein is found, together with its isomer zeaxanthin, in almost all the structures of the eye. Lutein and zeaxanthin are the only two dietary carotenoids selectively concentrated in the lens and in the macula, where they are the key components of the macular pigment (MP). An additional carotenoid present in the macula, meso-zeaxanthin, is a stereoisomer of lutein and zeaxanthin that is not naturally found in the human diet.
Epidemiological studies have shown that a daily intake of at least 6 mg of lutein plus zeaxanthin from dietary sources may decrease the risk of developing advanced age-related macular degeneration (AMD),1 the incidence of cataract2 and the need for cataract extraction.3,4 In studies using higher doses of lutein, administered alone or together with other antioxidants in a supplement form, the interventions were effective in increasing the macular pigment optical density (MPOD) in AMD patients and improving visual function in subjects suffering from AMD or cataract.5,6 These findings suggest that lutein and zeaxanthin may act as nutritional factors capable of modulating the processes implicated in the pathogenesis and progression of these degenerative eye diseases. Evidence of the beneficial effects of long-term supplementation with 10 mg lutein plus 2 mg zeaxanthin on the progression of advanced AMD, cataract and moderate vision loss is currently being investigated in the Age-related eye disease study 2 (AREDS2), a large-scale clinical trial conducted by the National Eye Institute of the US National Institutes of Health whose results are expected by 2013.7
The effects of lutein supplementation have also been explored in clinical trials conducted in patients with retinitis pigmentosa. They showed the ability of lutein to increase MPOD8,9 and slow the decline in the loss of visual field.9,10
In recent years, research interest has focused on the relationship between high daily intakes of lutein and zeaxanthin and the improvement in visual performance in healthy young adults. Observational studies have clearly shown that individuals with a higher density of MP are able to tolerate a higher intensity of glaring light and have significantly shorter photostress recovery times.11 These findings were strengthened by the results of an intervention study published in 2008, which showed that increasing MPOD through six months of supplementation with 10 mg lutein plus 2 mg zeaxanthin improved glare tolerance and reduced photostress recovery time.12 The benefits associated with lutein and zeaxanthin intake (and high MP density) are ascribed to particular characteristics of these carotenoids, which are:

  • the antioxidant activity, leading to a reduction of oxidative damage caused by reactive oxygen species and free radicals, which is especially important in the retina, a tissue that is particularly susceptible to oxidative stress; and
  • the ability to filter short wavelengths of visible light, associated with visual performance effects.13

Dietary Sources and Intakes

Like all the other carotenoids, lutein and zeaxanthin are not synthesised by humans. Their presence and concentration in serum and in the eye are entirely of dietary origin and can be raised by increasing intake, via diet and/or supplementation. Meso-zeaxanthin, however, is not obtained from the diet, nor is it found in serum, and has been shown to be formed through lutein metabolism, apparently exclusively within the macula.14
The richest source of lutein and zeaxanthin in the human diet is green leafy vegetables (such as kale, spinach and collards), corn and corn products and eggs – which are one of the most bioavailable sources of lutein and zeaxanthin due to the lack of lutein–matrix interaction observed in plants and the high lipid and cholesterol content of the yolk15 (see Figure 1). Most values for lutein and zeaxanthin are reported as total sum; however, green leafy vegetables contain very small or no amounts of zeaxanthin.16,17
Lutein and zeaxanthin exist in nature in two different chemical forms: the unesterified or ‘free’ form – such as in green leafy vegetables – and the esterified form – in which a fatty acid is attached to the hydroxyl groups at each end of the lutein (and zeaxanthin) molecule. The latter form is usually found in flowers and in very small amounts in yellow-orange vegetables and fruits. The human diet is predominantly composed of lutein in the free form and this is the only form that circulates in the serum and is deposited in the eye regardless of the type of lutein ingested.18,19
A diet rich in vegetables and fruits normally supplies an adequate level of lutein per day. However, the daily consumption of lutein and zeaxanthin in Western countries is generally modest, averaging only between 1 and 2.5 mg/day in the US20 and between 1.56 and 3.25 mg/day in Europe depending on the country.21 These amounts are well below the level of intake that is thought to be beneficial for eye health. Commercial ingredients containing lutein and zeaxanthin are on the market to increase the intake for people who are not ingesting sufficient quantities of these xanthophylls through their diet.

Lutein Absorption

Lutein is one of the six major carotenoids found in human blood. The presence of lutein in the blood varies considerably between individuals and may be influenced by external and host factors that can interfere with the different steps involved in its absorption: source of lutein ingested, duration of lutein intake, amount of fat in the diet, concomitant ingestion of fibres, nutritional status, genetic factors and age of the individual.22
To be deposited in the eye and thus provide its health benefits, lutein has to be absorbed by the body and circulated through the serum. Lutein is a lipophilic molecule and its absorption follows the same processes as other fat-soluble dietary compounds such as dietary lipids or vitamin E. Thus, the concomitant ingestion of some fat is necessary for its optimal absorption. Generally, after release from the food matrix into which the lutein is ingested and release into the lumen of the intestine, the lutein molecules are incorporated into mixed micelles formed from the dietary fats and bile acids present. Lutein is then absorbed by the mucosa of the small intestine via passive diffusion, incorporated into chylomicrons and transported via the lymphatic system to the liver. Finally, in the hepatocytes, lutein is incorporated into low-density and high-density lipoproteins and transported to target tissues.23 In the retina, a specific lutein-binding protein mediates the selective uptake of this carotenoid.24
One of the most critical factors influencing lutein absorption is the source of lutein ingested: its chemical form and the matrix in which the lutein is included. The nature of the source is of particular importance when increased lutein intake is obtained through supplementation.

Increase Bioavailability with FloraGLO® Lutein

FloraGLO Lutein (Kemin Health) is the leading lutein ingredient brand worldwide and is intended for inclusion in either dietary supplements, foods or beverages to increase the intake of lutein and zeaxanthin. It provides the same non-esterified form of lutein and zeaxanthin that is naturally found in vegetables. A pharmacokinetic study conducted in healthy volunteers has clearly demonstrated that the lutein from FloraGLO Lutein is absorbed unmodified by the body and circulates in the bloodstream.25 Intervention studies have confirmed the efficacy of supplementation with this patented ingredient to increase MPOD and improve visual performance in AMD patients and healthy subjects.5,12 The investigators of the AREDS2 chose FloraGLO Lutein as the source of lutein to be assessed in this important clinical trial.
Intake of supplements containing FloraGLO Lutein has been shown to increase serum lutein more than a similar dose of free lutein from green vegetables.26,27
Another topic of discussion in the scientific community deals with the possible differences in absorption of free lutein as compared to the esterified compound. Because only the free form is absorbed by the body, the fatty acids attached to the esterified form must be removed before absorption. Because this action, performed by gut enzymes not yet fully identified, does not seem to be 100 % efficient,28,29 there is reason to believe that lutein esters are less bioavailable than free lutein. Two small studies conducted to compare the absorption of lutein and lutein esters concluded that esterification does not impair lutein absorption; however, certain aspects of the design of these studies (including the amount of fat administered, duration of supplementation, product formulations and/or dose) do not allow clear conclusions to be drawn on this topic.15,30
A recently published intervention study provided a better understanding of the absorption of the different forms of lutein by comparing the serum lutein response resulting from 28 days of supplementation with FloraGLO Lutein with the response resulting from lutein esters provided in identical doses, galenic form and similar conditions.31
This randomised, double-blind parallel clinical trial, conducted with 72 healthy male and females volunteers, clearly confirmed the greater bioavailability of free lutein. Although both supplements increased serum lutein levels compared with baseline levels, supplementation with FloraGLO Lutein resulted in a statistically significant greater percentage increase in serum lutein levels (p=0.0054), a greater absolute (baseline subtracted) change in the serum lutein levels per mg of lutein dose administered (p=0.0011 at day 28) and a greater amount of lutein in the bloodstream as measured by serum lutein area under the curve (AUC(0–28d) ) (p=0.0187) (see Figure 2). Additionally, no lutein esters were detectable in the bloodstream.
Lutein in its crystalline form is very sensitive to oxidation, heat and humidity, therefore it is important to encapsulate it in a matrix to provide protection. The formulation technology used by the ingredient manufacturer for that purpose must ensure that:

  • the materials used are suitable for human consumption;
  • the ingredient can resist further processing (for example, inclusion in eye supplement tablets) so that the dose of lutein on the label is stable throughout the product’s shelf life; and
  • the lutein is released from the encapsulation matrix in the gut; this is of outmost importance, since it is a requirement for the lutein to be absorbed by the body.

A recent randomised, double-blind, cross-over study explored this critical point by comparing the bioavailability of two commercially available free lutein ingredients that differed in matrix characteristics: FloraGLO Lutein, which is microencapsulated in a starch matrix (Actilease™ technology, DSM Nutritional Products), and a free lutein incorporated into an alginate matrix. The study results, presented at the European Association for Vision and Eye Research conference in 2010,33 confirmed that not all lutein encapsulation forms are alike: the increase in lutein plasma AUC was 10 times higher following the single dose administration of 20 mg of FloraGLO Lutein compared with the same dose of free lutein incorporated into an alginate matrix.

Conclusions

The antioxidants and blue-light filtering properties of lutein, together with its selective accumulation in the retina, support its beneficial effects in eye health. Although no dietary reference has yet been set for lutein, data on beneficial effects observed in intervention trials support the daily intake of 10 mg of lutein, a dose that has been recognised to be safe.34,35 Since this carotenoid is not synthesised by the body and daily dietary consumption is generally low, increased consumption of lutein is recommended. Not all lutein ingredients are alike so, when recommending eye supplements to patients, in addition to looking for safe products, it is critical to ensure that the lutein ingredient used is absorbed properly by the body and has proven its efficacy in clinical trials. ■

Article Information:
Disclosure

Samanta Maci is an employee of Kemin Health.

Correspondence

Samanta Maci, Senior Manager Europe, Scientific Affairs and Technical Services, Kemin Health Europe, Campo Grande, 35-8ºD, 1700-087 Lisboa, Portugal. E: Samanta.Maci@kemin.com

Received

2011-09-06T00:00:00

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